Nitroimidazole

5-Nitroimidazole^[1]
Names
	Preferred IUPAC name 5-Nitro-1H-imidazole
Identifiers
CAS Number	3034-38-6 ;
3D model (JSmol)	Interactive image;
ChemSpider	10637918 ;
ECHA InfoCard	100.019.296
EC Number	221-224-7;
PubChem CID	18208;
UNII	Y8U32AZ5O7 ;
CompTox Dashboard (EPA)	DTXSID9062803 ;
	InChI InChI=1S/C3H3N3O2/c7-6(8)5-2-1-4-3-5/h1-3H Key: KUNMIWQQOPACSS-UHFFFAOYSA-N ;
	SMILES c1cn(cn1)[N+](=O)[O-];
Properties
Chemical formula	C3H3N3O2
Molar mass	113.076 g·mol−1
Melting point	303 °C (577 °F; 576 K) (decomposes)
Hazards
	GHS labelling:
Pictograms
Signal word	Warning
Hazard statements	H302
Precautionary statements	P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P321, P322, P330, P332+P313, P337+P313, P362, P363, P403+P233, P405, P501
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

Nitroimidazoles are the group of organic compounds consisting of an imidazole ring with at least one nitro group substituent. The term also refers to the class of antibiotics that have nitroimidazole in their structures.^[2] These antibiotics commonly include the 5-nitroimidazole positional isomer.

Synthesis

Imidazole undergoes a nitration reaction with a mixture of nitric acid and sulfuric acid to give 5-nitroimidazole.

Nitroimidazole antibiotics

From the chemistry perspective, nitroimidazole antibiotics can be classified according to the location of the nitro functional group. Structures with names 4- and 5-nitroimidazole are equivalent from the perspective of drugs since these tautomers readily interconvert. Drugs of the 5-nitro variety include metronidazole, tinidazole, nimorazole, dimetridazole, pretomanid, ornidazole, megazol, and azanidazole. Drugs based on 2-nitroimidazoles include benznidazole and azomycin.^[3]

Nitroimidazole antibiotics have been used to combat anaerobic bacterial and parasitic infections.^[4] Perhaps the most common example is metronidazole. Other heterocycles such as nitrothiazoles (thiazole) are also used for this purpose. Nitroheterocycles may be reductively activated in hypoxic cells, and then undergo redox recycling or decompose to toxic products.^[5]

References

^ 4-Nitroimidazole at Sigma-Aldrich
^ Edwards, David I. (1993). "Nitroimidazole drugs-action and resistance mechanisms I. Mechanism of action". Journal of Antimicrobial Chemotherapy. 31 (1): 9–20. doi:10.1093/jac/31.1.9. PMID 8444678.
^ Jenks, Peter J. (2010-01-01), Finch, Roger G.; Greenwood, David; Norrby, S. Ragnar; Whitley, Richard J. (eds.), "CHAPTER 24 - Nitroimidazoles", Antibiotic and Chemotherapy (Ninth Edition), London: W.B. Saunders, pp. 292–300, doi:10.1016/b978-0-7020-4064-1.00024-5, ISBN 978-0-7020-4064-1, retrieved 2023-10-18
^ Mital A (2009). "Synthetic Nitroimidazoles: Biological Activities and Mutagenicity Relationships". Sci Pharm. 77 (3): 497–520. doi:10.3797/scipharm.0907-14.
^ Juchau, MR (1989). "Bioactivation in chemical teratogenesis". Annu. Rev. Pharmacol. Toxicol. 29: 165–167. doi:10.1146/annurev.pa.29.040189.001121. PMID 2658769.

[1] 4-Nitroimidazole at Sigma-Aldrich

[2] Edwards, David I. (1993). "Nitroimidazole drugs-action and resistance mechanisms I. Mechanism of action". Journal of Antimicrobial Chemotherapy. 31 (1): 9–20. doi:10.1093/jac/31.1.9. PMID 8444678.

[3] Jenks, Peter J. (2010-01-01), Finch, Roger G.; Greenwood, David; Norrby, S. Ragnar; Whitley, Richard J. (eds.), "CHAPTER 24 - Nitroimidazoles", Antibiotic and Chemotherapy (Ninth Edition), London: W.B. Saunders, pp. 292–300, doi:10.1016/b978-0-7020-4064-1.00024-5, ISBN 978-0-7020-4064-1, retrieved 2023-10-18

[Mital2009-4] Mital A (2009). "Synthetic Nitroimidazoles: Biological Activities and Mutagenicity Relationships". Sci Pharm. 77 (3): 497–520. doi:10.3797/scipharm.0907-14.

[5] Juchau, MR (1989). "Bioactivation in chemical teratogenesis". Annu. Rev. Pharmacol. Toxicol. 29: 165–167. doi:10.1146/annurev.pa.29.040189.001121. PMID 2658769.

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